JP2000169385A - Internal liquid pharmaceutical preparation - Google Patents

Internal liquid pharmaceutical preparation

Info

Publication number
JP2000169385A
JP2000169385A JP10351800A JP35180098A JP2000169385A JP 2000169385 A JP2000169385 A JP 2000169385A JP 10351800 A JP10351800 A JP 10351800A JP 35180098 A JP35180098 A JP 35180098A JP 2000169385 A JP2000169385 A JP 2000169385A
Authority
JP
Japan
Prior art keywords
iron
component
mmol
citrate
xylitol
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP10351800A
Other languages
Japanese (ja)
Inventor
Hiroshi Nakano
洋 中野
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Taisho Pharmaceutical Co Ltd
Original Assignee
Taisho Pharmaceutical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Taisho Pharmaceutical Co Ltd filed Critical Taisho Pharmaceutical Co Ltd
Priority to JP10351800A priority Critical patent/JP2000169385A/en
Publication of JP2000169385A publication Critical patent/JP2000169385A/en
Pending legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To obtain an internal liquid pharmaceutical preparation that is readily takable, while its metallic taste originating from iron is masked, and is useful for treatment and prevention of anemia, poor circulation or the like by using iron components, rehmanniae radix (a kind of Chinese medicine) and xylitol. SOLUTION: This internal liquid pharmaceutical preparation includes (A) an iron component, preferably iron citrate, ammonium iron citrate, sodium iron citrate or the like, (B) rehmanniae radix and (C) xylitol. In a preferred embodiment, the amount of the component (A) is 0.05-50 mmol/L calculated as iron, that of the component (B) is 40-2,000 mg every dose calculated as the original herb, and that of the component (C) is >=20 mmol per 1 mmol of the iron in the component (A). This liquid preparation can be applied to internal liquid of drugs and quasi drugs, for example, drinkable preparation, syrups, and the like and a variety of beverages, for example, health drinks or the like.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明が属する技術分野】本発明は、鉄成分と地黄を配
合した液剤において鉄由来の金属味が軽減された内服液
剤に関するものであり、医薬、食品の分野に応用できる
ものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a liquid preparation containing an iron component and ground yellow in which the metallic taste derived from iron is reduced, and is applicable to the fields of medicine and food.

【0002】[0002]

【従来の技術】鉄は、主に血液中のヘモグロビン、筋肉
中のミオグロビン、肝臓のフェリチンなど、生体内に広
く分布し、不足すると貧血や倦怠感などの症状をひき起
こす。また、地黄は、血糖下降作用、抗血管内凝固作
用、血流改善効果などがあり、冷え性などの改善に効果
がある生薬である。貧血や冷え性などは女性に多くみら
れる症状であり、従って鉄と地黄を同時に配合する薬剤
は特に女性用の医薬として有用である。しかしながら、
鉄成分を内服液剤に配合した場合には、その独特の金属
味ゆえに服用しにくいという欠点があった。
2. Description of the Related Art Iron is widely distributed in living organisms, such as hemoglobin in blood, myoglobin in muscle, and ferritin in liver. If iron is insufficient, it causes symptoms such as anemia and malaise. In addition, ground yellow has a blood glucose lowering action, an anti-intravascular coagulation action, a blood flow improving effect, and the like, and is a crude drug that is effective in improving coldness and the like. Anemia, chilliness and the like are symptoms that are common in women. Therefore, a drug containing iron and ground yellow at the same time is particularly useful as a medicine for women. However,
When an iron component is incorporated into an oral solution, there is a drawback that it is difficult to take due to its unique metallic taste.

【0003】このような鉄由来の金属味を改善する方法
としては、フルーツジュースを配合する方法(特開昭6
4−86858号公報)、アルコール成分を配合する方
法(特開平4−27369号公報)、香料を配合する方
法などが知られているが、必ずしも十分なものではな
い。
[0003] As a method of improving such metallic taste derived from iron, a method of blending fruit juice (Japanese Patent Application Laid-Open No.
JP-A-4-86858), a method of blending an alcohol component (JP-A-4-27369), and a method of blending a fragrance are known, but are not necessarily sufficient.

【0004】一方、地黄にはそれ自身に金属味をマスキ
ングする効果があり、鉄成分を含む内服液剤に地黄を配
合することは有用である。しかしながら、低濃度の鉄成
分を含む内服液剤の場合には有用であっても、高濃度の
場合には必ずしも充分なマスキング効果が得られないと
いう問題点がある。
On the other hand, ground yellow has an effect of masking metallic taste to itself, and it is useful to mix ground yellow with an oral solution containing an iron component. However, there is a problem that even if the liquid preparation containing an iron component at a low concentration is useful, a sufficient masking effect cannot always be obtained at a high concentration.

【0005】[0005]

【発明が解決しようとする課題】本発明の目的は、鉄成
分と地黄を配合し、鉄由来の金属味をマスキングした、
貧血や冷え性などの治療又は予防に対して極めて有効な
内服液剤を提供することである。
SUMMARY OF THE INVENTION An object of the present invention is to mix an iron component and ground yellow to mask the metallic taste derived from iron.
It is an object of the present invention to provide an oral solution which is extremely effective for treating or preventing anemia and chilliness.

【0006】[0006]

【課題を解決するための手段】本発明者らは、上記目的
を達するため鋭意研究を進めた結果、鉄成分と地黄を配
合した内服液剤において新たにキシリトールを配合する
ことにより課題を解決することを見いだし、本発明を完
成した。すなわち、本発明は鉄成分、地黄及びキシリト
ールを含有することを特徴とする内服液剤である。
Means for Solving the Problems The present inventors have made intensive studies to achieve the above object, and as a result, have solved the problem by adding a new xylitol to an oral solution containing an iron component and ground yellow. And completed the present invention. That is, the present invention is an oral liquid preparation characterized by containing an iron component, ground yellow and xylitol.

【0007】[0007]

【発明の実施の形態】本発明において、鉄成分はクエン
酸鉄、クエン酸鉄アンモニウム、クエン酸鉄ナトリウ
ム、グルコン酸第一鉄、乳酸鉄、ピロリン酸第一鉄、ピ
ロリン酸第二鉄、硫酸第一鉄、塩化第二鉄など、内服液
剤に配合可能な鉄含有化合物であれば特に限定されない
が、クエン酸鉄、クエン酸鉄アンモニウム及びクエン酸
鉄ナトリウム、グルコン酸第一鉄でより本発明の効果が
発揮され、更にクエン酸鉄アンモニウムでより本発明の
効果が発揮される。鉄成分は、鉄量として50mmol/L以
下の割合で配合した場合本発明の効果が発現するが、鉄
量が0.05mmol/L以下の薄い領域では、本発明に依ら
ずマスキングが可能であり、濃い領域では効果が低くな
る。好ましくは0.1〜30mmol/Lの範囲であ
る。
BEST MODE FOR CARRYING OUT THE INVENTION In the present invention, iron components are iron citrate, iron ammonium citrate, iron sodium citrate, ferrous gluconate, iron lactate, ferrous pyrophosphate, ferric pyrophosphate, and sulfuric acid. There is no particular limitation as long as it is an iron-containing compound, such as ferrous iron or ferric chloride, which can be blended in the oral liquid, but the present invention is more preferable with iron citrate, iron ammonium citrate and sodium iron citrate, and ferrous gluconate. And the effect of the present invention is further exhibited by ammonium iron citrate. Although the effect of the present invention is exhibited when the iron component is blended at a rate of 50 mmol / L or less as the iron content, masking is possible regardless of the present invention in a thin region where the iron content is 0.05 mmol / L or less. In a dark area, the effect is low. Preferably, it is in the range of 0.1 to 30 mmol / L.

【0008】本発明に用いる地黄は生地黄、鮮地黄、乾
地黄、熟地黄など、及びそられを原料とし通常の方法に
より製造された乾燥エキス、軟エキス、流エキス、抽出
液であり、一般に市販されているものも使用することが
できる。地黄の配合量は、それ自身に薬効及びマスキン
グ効果があることから、原生薬換算量として10〜40
00mg、好ましくは40〜2000mgを1回服用量とし
て配合することができる。10mg以下だとその効果が期
待できず、4000mgを越えて配合することは地黄自身
の味が強く風味が損なわれるからである。
[0008] The ground yellow used in the present invention is dough yellow, fresh ground yellow, dry ground yellow, mature ground yellow, etc., and dry extracts, soft extracts, flow extracts, and extracts prepared from the raw materials by the usual methods. Commercially available ones can also be used. The amount of ground yellow is 10 to 40 as a crude drug equivalent, since it has a medicinal effect and a masking effect by itself.
00 mg, preferably 40-2000 mg, can be formulated as a single dose. If the amount is less than 10 mg, the effect cannot be expected, and if it exceeds 4000 mg, the ground yellow itself has a strong taste and the flavor is impaired.

【0009】キシリトールは、鉄量1mmolに対しキシリ
トール20mmol以上配合することにより鉄と地黄配合下
における鉄由来の金属味をマスキングできるが、好まし
くは30mmol以上である。また、キシリトールは緩下作
用があることから、1回服用量は20g以下が好まし
い。
Xylitol can mask a metallic taste derived from iron in a mixture of iron and ground yellow by adding 20 mmol or more of xylitol to 1 mmol of iron, but is preferably 30 mmol or more. In addition, since xylitol has a laxative effect, a single dose is preferably 20 g or less.

【0010】また、本発明の内服液剤には他にビタミン
類、例えばビタミンB群、ビタミンC類などの水溶性ビ
タミン、ビタミンA類、ビタミンD類、ビタミンE類な
どの脂溶性ビタミンなどを含んでも良い。これらのビタ
ミン類は、一種又は二種以上使用できる。
The oral liquid preparation of the present invention also contains vitamins, for example, water-soluble vitamins such as vitamin B group and vitamin C, and fat-soluble vitamins such as vitamin A, vitamin D and vitamin E. But it is good. One or more of these vitamins can be used.

【0011】本発明の内服液剤のpHは通常2〜7程
度、好ましくは2.5〜6程度である。内服液剤のpH
は繁用のpH調整剤を用いて調整できる。pH調整剤と
しては、例えばクエン酸、リンゴ酸、酒石酸、フマル
酸、乳酸、コハク酸、アスコルビン酸、酢酸などの有機
酸及びそれらの塩類、塩酸、リン酸などの無機酸及びそ
れらの塩類などが挙げられる。これらのpH調整剤は一
種又は二種以上使用できる。
The pH of the liquid preparation of the present invention is usually about 2 to 7, preferably about 2.5 to 6. PH of oral solution
Can be adjusted using a conventional pH adjuster. Examples of the pH adjuster include organic acids and salts thereof such as citric acid, malic acid, tartaric acid, fumaric acid, lactic acid, succinic acid, ascorbic acid, and acetic acid; and inorganic acids and salts thereof such as hydrochloric acid and phosphoric acid. No. One or more of these pH adjusters can be used.

【0012】また、本発明の内服液剤には、その他の成
分としてミネラル、アミノ酸及びその塩類、生薬及び生
薬抽出物、甘味剤、保存剤、矯味剤、着香剤、着色剤な
ど、内服液剤一般に使用される成分を配合することがで
きる。
The oral liquid preparation of the present invention generally contains, as other components, minerals, amino acids and salts thereof, crude drugs and crude drug extracts, sweeteners, preservatives, flavoring agents, flavoring agents, coloring agents and the like. The components used can be blended.

【0013】本発明かかわる内服液剤は、常法により調
製でき、その方法は特に制限はされないが、通常、各成
分を規定量以下の精製水にて混合し、規定量に容量調整
し、必要に応じて濾過、滅菌処理をすることにより得ら
れる。なお、脂溶性ビタミンを含むときは、通常用いら
れる界面活性剤又は可溶化剤により乳化又は可溶化して
もよく、また分散剤を用いて懸濁させても良い。
The liquid preparation for internal use according to the present invention can be prepared by a conventional method, and the method is not particularly limited. Usually, each component is mixed with a specified amount or less of purified water, and the volume is adjusted to the specified amount. It is obtained by performing filtration and sterilization as appropriate. When a fat-soluble vitamin is contained, the fat-soluble vitamin may be emulsified or solubilized with a commonly used surfactant or solubilizer, or may be suspended with a dispersant.

【0014】本発明の内服液剤は、例えばドリンク剤、
シロップ剤などの医薬品や医薬部外品の内服液剤、健康
飲料などの各種飲料に適用できる。
The oral liquid preparation of the present invention is, for example, a drink preparation,
The present invention can be applied to various kinds of beverages such as medicines such as syrups, oral liquids of quasi-drugs, and health drinks.

【0015】[0015]

【発明の効果】鉄成分と地黄を配合した内服液剤におい
て、更にキシリトールを配合することにより鉄由来の金
属味を有効に軽減し服用し易い内服液剤を提供できるこ
とを見出した。
According to the present invention, it has been found that, by further mixing xylitol in an oral solution containing an iron component and ground yellow, an oral solution which can effectively reduce the metallic taste derived from iron and is easy to take can be provided.

【0016】[0016]

【実施例】次に、本発明を実施例及び試験例を挙げて詳
細に説明する。 実施例1 クエン酸鉄アンモニウム 40 mg 地黄エキス 200 mg(原生薬換算) キシリトール 2000 mg 精製水 (全量) 100 mL (鉄量として約1.2mmol/L) 上記成分を混合溶解し液剤を得た。
Next, the present invention will be described in detail with reference to examples and test examples. Example 1 Ammonium iron citrate 40 mg Ground yellow extract 200 mg (equivalent to crude drug) Xylitol 2000 mg Purified water (total) 100 mL (about 1.2 mmol / L as iron) The above components were mixed and dissolved to obtain a liquid preparation.

【0017】 実施例2 クエン酸鉄アンモニウム 40 mg 地黄エキス 200 mg(原生薬換算) キシリトール 2000 mg リンゴ酸 適量 (pH4) 精製水 (全量) 100 mL (鉄量として約1.2mmol/L) 上記成分を混合溶解し液剤を得た。Example 2 Ammonium iron citrate 40 mg Ground yellow extract 200 mg (converted to crude drug) Xylitol 2000 mg Malic acid Suitable amount (pH 4) Purified water (total amount) 100 mL (about 1.2 mmol / L as iron) Were mixed and dissolved to obtain a liquid preparation.

【0018】 実施例3 クエン酸鉄アンモニウム 100 mg 地黄エキス 500 mg(原生薬換算) キシリトール 10000 mg 精製水 (全量) 100 mL (鉄量として約3.0mmol/L) 上記成分を混合溶解し液剤を得た。Example 3 Ammonium iron citrate 100 mg Ground yellow extract 500 mg (equivalent to crude drug) Xylitol 10,000 mg Purified water (total amount) 100 mL (about 3.0 mmol / L as iron amount) Obtained.

【0019】 実施例4 クエン酸鉄アンモニウム 100 mg 地黄エキス 400 mg(原生薬換算) キシリトール 6000 mg リンゴ酸 適量 (pH4) 精製水 (全量) 100 mL (鉄量として約3.0mmol/L) 上記成分を混合溶解し液剤を得た。Example 4 Ammonium iron citrate 100 mg Ground yellow extract 400 mg (converted to crude drug) Xylitol 6000 mg Malic acid Suitable amount (pH 4) Purified water (total amount) 100 mL (about 3.0 mmol / L as iron) Were mixed and dissolved to obtain a liquid preparation.

【0020】 実施例5 クエン酸鉄アンモニウム 60 mg 地黄エキス 200 mg(原生薬換算) 硝酸チアミン 5 mg リン酸リボフラビンナトリウム 10 mg 塩酸ピリドキシン 10 mg アミノエチルスルホン酸 1500 mg L−アスパラギン酸マグネシウム 1200 mg グルコン酸カルシウム 2500 mg ニコチン酸アミド 20 mg イノシトール 100 mg 無水カフェイン 50 mg ヨクイニン流エキス 2000 mg(原生薬換算) キシリトール 5000 mg 砂糖 5000 mg エリスリトール 1000 mg 安息香酸ナトリウム 70 mg パラオキシ安息香酸ブチル 5 mg パラオキシ安息香酸プロピル 5 mg DL−リンゴ酸 500 mg クエン酸 適量(pH4) ミックスフルーツフレーバー 微量 精製水 (全量) 100 mL (鉄量として1.8mmol/L) 上記成分を混合溶解し液剤を得た。Example 5 Ammonium iron citrate 60 mg Ground yellow extract 200 mg (converted to crude drug) Thiamine nitrate 5 mg Riboflavin sodium phosphate 10 mg Pyridoxine hydrochloride 10 mg Aminoethylsulfonic acid 1500 mg Magnesium L-aspartate 1200 mg Gluconic acid Calcium 2500 mg Nicotinamide 20 mg Inositol 100 mg Anhydrous caffeine 50 mg Yokuinin flow extract 2000 mg (converted to crude drug) Xylitol 5000 mg Sugar 5000 mg Erythritol 1000 mg Sodium benzoate 70 mg Butyl benzoate Propyl benzoate 5 mg Propyl paraoxybenzoate 5 mg DL-malic acid 500 mg Citric acid Appropriate amount (pH 4) Mixed fruit flavor Trace amount Purified water (Total amount) ) 100 mL (1.8 mmol / L as iron amount) The above components were mixed and dissolved to obtain a liquid preparation.

【0021】 比較例1 クエン酸鉄アンモニウム 20 mg 地黄エキス 100 mg(原生薬換算) 精製水 (全量) 100 mL (鉄量として約0.6mmol/L) 上記成分を混合溶解し液剤を得た。Comparative Example 1 Ammonium iron citrate 20 mg Ground yellow extract 100 mg (in terms of crude drug) Purified water (total amount) 100 mL (about 0.6 mmol / L as iron amount) The above components were mixed and dissolved to obtain a liquid preparation.

【0022】 比較例2 クエン酸鉄アンモニウム 40 mg 地黄エキス 200 mg(原生薬換算) リンゴ酸 適量 (pH4) 精製水 (全量) 100 mL (鉄量として約1.8mmol/L) 上記成分を混合溶解し液剤を得た。Comparative Example 2 Ammonium iron citrate 40 mg Ground yellow extract 200 mg (converted to crude drug) Malic acid Suitable amount (pH 4) Purified water (total amount) 100 mL (about 1.8 mmol / L as iron amount) A solution was obtained.

【0023】試験例 上記の実施例1〜4、比較例1及び比較例2の6種類の
鉄成分を配合した液剤について、20人のパネラーによ
り金属味の程度を官能評価した。なお、金属味の評価は
以下の6段階評価で行い、それぞれ平均点を算出した。
Test Examples The liquids containing the six iron components of Examples 1 to 4 and Comparative Examples 1 and 2 were organoleptically evaluated for the degree of metallic taste by 20 panelists. In addition, the evaluation of metal taste was performed by the following six-step evaluation, and the average score was calculated for each.

【0024】 評価1:金属味をかなり強く感じる(5点) 評価2:金属味を強く感じる (4点) 評価3:金属味をやや強く感じる (3点) 評価4:金属味を感じる (2点) 評価5:金属味をやや弱く感じる (1点) 評価6:金属味を感じない (0点)。Evaluation 1: Metallic taste is strongly felt (5 points) Evaluation 2: Metallic taste is strongly felt (4 points) Evaluation 3: Metallic taste is somewhat strong (3 points) Evaluation 4: Metallic taste is felt (2 points) Evaluation 5: Metallic taste is slightly weakened (1 point) Evaluation 6: Metallic taste is not felt (0 point).

【0025】結果を表1に示した。表1より明らかなよ
うに、キシリトールの添加により、鉄由来の金属味が顕
著に軽減されることが証明された。
The results are shown in Table 1. As is clear from Table 1, it was proved that the addition of xylitol significantly reduced the metallic taste derived from iron.

【0026】[0026]

【表1】 [Table 1]

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) A61K 47/10 A61K 47/10 L Fターム(参考) 4C076 AA12 BB01 CC11 CC14 CC21 DD30E DD38T DD41A DD43A EE58T FF52 4C086 AA01 AA02 GA13 HA11 HA20 MA03 MA05 MA17 MA52 NA09 ZA36 ZA54 ZA55 ZC21 ZC35 4C088 AB37 AC13 BA08 MA02 MA17 MA52 NA09 ZA36 ZA54 ZA55 ZC21 ZC35 4C206 AA01 AA02 CA05 DB03 DB27 JB11 KA13 MA03 MA05 MA37 MA72 NA09 ZA36 ZA54 ZA55 ZC21 ZC35 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification symbol FI theme coat ゛ (Reference) A61K 47/10 A61K 47/10 LF term (Reference) 4C076 AA12 BB01 CC11 CC14 CC21 DD30E DD38T DD41A DD43A EE58T FF52 4C086 AA01 AA02 GA13 HA11 HA20 MA03 MA05 MA17 MA52 NA09 ZA36 ZA54 ZA55 ZC21 ZC35 4C088 AB37 AC13 BA08 MA02 MA17 MA52 NA09 ZA36 ZA54 ZA55 ZC21 ZC35 4C206 AA01 AA02 CA05 DB03 DB27 JB11 KA13 MA03 Z0537

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 鉄成分、地黄及びキシリトールを含有す
ることを特徴とする内服液剤。
1. An oral solution containing an iron component, ground yellow and xylitol.
【請求項2】 鉄成分の含有量が鉄量として0.05〜
50mmol/Lである請求項1に記載の内服液剤。
2. The iron content is 0.05 to 5% in terms of iron content.
The oral liquid preparation according to claim 1, wherein the amount is 50 mmol / L.
【請求項3】 鉄成分が鉄量として1mmolあたりキシリ
トール20mmol以上配合することを特徴とする請求項1
又は2に記載の内服液剤。
3. The method according to claim 1, wherein the iron component comprises at least 20 mmol of xylitol per 1 mmol of iron.
Or the oral liquid preparation according to 2.
【請求項4】 鉄成分がクエン酸鉄、クエン酸鉄アンモ
ニウム、クエン酸鉄ナトリウム及びグルコン酸第一鉄か
ら選ばれる少なくとも1種である請求項1〜3のいずれ
かに記載の内服液剤。
4. The oral liquid preparation according to claim 1, wherein the iron component is at least one selected from iron citrate, iron ammonium citrate, sodium iron citrate and ferrous gluconate.
JP10351800A 1998-12-10 1998-12-10 Internal liquid pharmaceutical preparation Pending JP2000169385A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10351800A JP2000169385A (en) 1998-12-10 1998-12-10 Internal liquid pharmaceutical preparation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10351800A JP2000169385A (en) 1998-12-10 1998-12-10 Internal liquid pharmaceutical preparation

Publications (1)

Publication Number Publication Date
JP2000169385A true JP2000169385A (en) 2000-06-20

Family

ID=18419701

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10351800A Pending JP2000169385A (en) 1998-12-10 1998-12-10 Internal liquid pharmaceutical preparation

Country Status (1)

Country Link
JP (1) JP2000169385A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002080347A (en) * 2000-09-04 2002-03-19 Taisho Pharmaceut Co Ltd Oral liquid medicine formulated with iron compound
WO2003024466A1 (en) * 2001-09-13 2003-03-27 Wakunaga Pharmaceutical Co., Ltd. Liquid preparation containing crude-drug extract
JP2005255653A (en) * 2004-03-15 2005-09-22 Taisho Pharmaceut Co Ltd Internal liquid medicine formulated with iron compound
WO2010004916A1 (en) * 2008-07-08 2010-01-14 株式会社ゲノム創薬研究所 Hypoglycemic agent, and food or beverage for prevention of diabetes or amelioration of condition of diabetes comprising same
JP2020002043A (en) * 2018-06-27 2020-01-09 小林製薬株式会社 Pharmaceutical composition

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06305976A (en) * 1993-02-24 1994-11-01 Taisho Pharmaceut Co Ltd Blood flow improver
JPH09194356A (en) * 1996-01-18 1997-07-29 Taisho Pharmaceut Co Ltd Internal liquid preparation compounded with iron compound
WO1998005312A1 (en) * 1996-08-07 1998-02-12 Ascent Pediatrics, Inc. Pleasant-tasting aqueous liquid composition of a bitter-tasting drug
JPH10306038A (en) * 1997-05-07 1998-11-17 Taisho Pharmaceut Co Ltd Bromhexine-containing solution
JPH111436A (en) * 1997-06-13 1999-01-06 Taisho Pharmaceut Co Ltd Iron-containing liquid agent
JPH11180840A (en) * 1997-12-22 1999-07-06 Lion Corp Xylitol-containing tablet
JP2002502817A (en) * 1998-02-03 2002-01-29 ラボラトワール イノテラ,ソシエテ アノニム Tablets containing iron as an active ingredient for chewing and licking

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06305976A (en) * 1993-02-24 1994-11-01 Taisho Pharmaceut Co Ltd Blood flow improver
JPH09194356A (en) * 1996-01-18 1997-07-29 Taisho Pharmaceut Co Ltd Internal liquid preparation compounded with iron compound
WO1998005312A1 (en) * 1996-08-07 1998-02-12 Ascent Pediatrics, Inc. Pleasant-tasting aqueous liquid composition of a bitter-tasting drug
JPH10306038A (en) * 1997-05-07 1998-11-17 Taisho Pharmaceut Co Ltd Bromhexine-containing solution
JPH111436A (en) * 1997-06-13 1999-01-06 Taisho Pharmaceut Co Ltd Iron-containing liquid agent
JPH11180840A (en) * 1997-12-22 1999-07-06 Lion Corp Xylitol-containing tablet
JP2002502817A (en) * 1998-02-03 2002-01-29 ラボラトワール イノテラ,ソシエテ アノニム Tablets containing iron as an active ingredient for chewing and licking

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002080347A (en) * 2000-09-04 2002-03-19 Taisho Pharmaceut Co Ltd Oral liquid medicine formulated with iron compound
WO2003024466A1 (en) * 2001-09-13 2003-03-27 Wakunaga Pharmaceutical Co., Ltd. Liquid preparation containing crude-drug extract
US7651706B2 (en) 2001-09-13 2010-01-26 Wakunaga Pharmaceutical Co., Ltd. Liquid preparation containing crude-drug extract
JP2005255653A (en) * 2004-03-15 2005-09-22 Taisho Pharmaceut Co Ltd Internal liquid medicine formulated with iron compound
WO2010004916A1 (en) * 2008-07-08 2010-01-14 株式会社ゲノム創薬研究所 Hypoglycemic agent, and food or beverage for prevention of diabetes or amelioration of condition of diabetes comprising same
JP5897796B2 (en) * 2008-07-08 2016-03-30 株式会社ゲノム創薬研究所 Hypoglycemic agent and food and drink for preventing diabetes or improving symptoms comprising the same
JP2020002043A (en) * 2018-06-27 2020-01-09 小林製薬株式会社 Pharmaceutical composition
JP7360784B2 (en) 2018-06-27 2023-10-13 小林製薬株式会社 pharmaceutical composition

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